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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Salivary Gland Diseases (D012466)
..Starting node ..Parotid Salivary Glands, Polycystic Disease of (C563951)
Child Nodes:
Sister Nodes:
..Aplasia of Lacrimal and Salivary Glands (C562407)
..Mikulicz' Disease (D008882)
..Parotid Diseases (D010305) 7
..Parotid Salivary Glands, Polycystic Disease of (C563951)
..Salivary Calculi (D020792) 2
..Salivary Gland Fistula (D012467)
..Salivary Gland Neoplasms (D012468) 6
..Sialadenitis (D012793) 6
..Sialometaplasia, Necrotizing (D012797)
..Sialorrhea (D012798)
..Submandibular Gland Diseases (D013364) 1
..Tunglang Savage Bellman syndrome (C536927)
..Xerostomia (D014987) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

8682

Name:

Parotid Salivary Glands, Polycystic Disease of

Definition:

Alternative IDs:

ParentIDs:

MESH:D012466

TreeNumbers:

C07.465.815/C563951

Synonyms:

Slim Mappings:

Mouth disease

Reference:

MedGen: C563951
MeSH: C563951
OMIM: 600343;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0000153	Abnormality of the mouth
3	HP:0000924	Abnormality of the skeletal system

Disease Causing ClinVar Variants